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Results: 1 to 17 of 17

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Athabaskan brainstem dysgenesis syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism Spectrum Disorders Sequencing Panel with CNV Detection

PreventionGenetics
United States
102108
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Congenital Fibrosis of Extraocular Muscles (Ocular Motility Disorder) or Strabismus Syndromes Sequencing Panel with CNV Detection

PreventionGenetics
United States
1110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Neurodevelopment-Expanded

Ambry Genetics
United States
308196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IDNext

Ambry Genetics
United States
221140
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext: Neuro

Ambry Genetics
United States
308196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism Spectrum Disorders (Expanded Panel) , Panel Massive Sequencing (NGS) 77 Genes

Reference Laboratory Genetics
Spain
8677
  • C Sequence analysis of the entire coding region

Congenital Central Hypoventilation Syndrome: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
117
  • D Deletion/duplication analysis

Autism

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2528
  • C Sequence analysis of the entire coding region

Athabaskan brainstem dysgenesis syndrome (sequence analysis of HOXA1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

HOXA1

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Central Hypoventilation Syndrome: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
117
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
177100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HOXA1-Related Disorders

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Autism/Intellectual Disability/Multiple Anomalies

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
11389
  • C Sequence analysis of the entire coding region

HOXA1-related syndromes, Athabaskan brainstem dysgenesis syndrome, Bosley-Salih-Alorainy syndrome

Engle Laboratory Boston Children's Hospital
United States
21
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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